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Browse result for Primary hyperoxaluria

※ introduction

    Primary hyperoxaluria is a rare condition (autosomal recessive), resulting in increased excretion of oxalate (up to 600 mg a day from normal 50 mg a day), with oxalate stones being common.

Reference
Wiki: Primary hyperoxaluria



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD04477P21549189
AGXT
Alanine--glyoxylate aminotransferase
Homo sapiens
PTMD14017Q9UBQ79380
GRHPR
Glyoxylate reductase/hydroxypyruvate reductase
Homo sapiens